MI HB4663

Requires healthcare licensees and registrants providing prenatal care, postnatal care, or genetic counseling to provide written information about Down syndrome when test results or screenings indicate a high likelihood or presence of Down syndrome in a fetus or newborn.

Mandates the Department of Health and Human Services develop and distribute written information on Down syndrome that includes clinical course description, treatment and therapy options, life expectancies, and contact information for support services and Down syndrome organizations.

Requires the written information to be reviewed by medical experts and be culturally and linguistically appropriate for caregivers of individuals with Down syndrome.

Directs the Department of Health and Human Services to annually update the Down syndrome information and make it available on the department's website.

Allows Down syndrome organizations to request that the department post their contact information on the department's website alongside the Down syndrome resources.